University Senior Lecturer
Division of Virology
University of Cambridge
Tennis Court Road
Virus assembly and egress
Herpesviruses are large (~200nm) and complex enveloped dsDNA viruses that are ubiquitous pathogens of vertebrates and establish life-long latent infections in their hosts. Infections by the nine known human herpesviruses are associated with many serious diseases including certain lymphomas and life-threatening conditions in immuno-compromised patients. The assembly of herpesviruses is known to involve the budding of nucleocapsids, together with the complex layer of tegument proteins, at membranes derived from post-Golgi endocytic compartments. Once formed, the membrane-bound compartments containing the mature virions undergo exocytosis to release infectious viruses from the cell.
Polyomaviruses are small (~45nm) non-enveloped dsDNA viruses that are ubiquitous pathogens in humans and can establish life-long persistent infections with periodic virus shedding. While polyomavirus infections are generally benign in immuno-competent hosts they are known to cause serious disease in immuno-compromised patients including haemorrhagic cystitis, polyomavirus-associated nephropathy, Merkel cell carcinoma, and progressive multifocal leukoencephalopathy.
Examples of current ongoing projects in the lab are:
- Host cell modulation by herpesvirus tegument proteins
- Cellular pathways involved in polyomavirus egress
- Viral and cellular mechanisms of herpesvirus secretion
- Super-resolution microscopy imaging of the structure and assembly of viruses in cells
- Host cell modulation by polyomavirus infection
- Post doctoral research associate:
Dr Tim Soh
- Graduate Students:
Laura Williamson, Firoz Ahmed, Yunhui Zhuang
- Chief Research Laboratory Technician:
- Albecka A, Owen DJ, Ivanova L, Brun J, Liman R, Davies L, Ahmed MF, Colaco S, Hollinshead M, Graham SC, Crump CM (2017) Dual Function of the pUL7-pUL51 Tegument Protein Complex in Herpes Simplex Virus 1 Infection. J Virol. 91(2) pii: e02196-16
- Albecka A, Laine RF, Janssen AFJ, Kaminski CF, Crump CM. (2016) HSV-1 glycoproteins are delivered to virus assembly sites through dynamin-dependent endocytosis. Traffic, 17(1):21-39. doi: 10.1111/tra.12340
- Evans GL, Caller LG, Foster V, Crump CM. (2015) Anion homeostasis is important for non-lytic release of BK polyomavirus from infected cells. Open Biol. 5: 150041. http://dx.doi.org/10.1098/rsob.150041
- Lau SY, Crump CM. (2015) HSV-1 gM and the gK/pUL20 complex are important for the localization of gD and gH/L to viral assembly sites. Viruses. Mar 4;7(3):915-38.
- Laine RF, Albecka A, van de Linde S, Rees EJ, Crump CM, Kaminski CF. (2015) Structural analysis of herpes simplex virus by optical super-resolution imaging. Nat Commun. Jan 22;6:5980